A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032751



Internal ID89528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43341247..43349504hg38UCSC Ensembl
chr10:43836695..43844952hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg388258
hg198258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032751
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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